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Phentermine Hydrochloride - 51224-202-50 - (Phentermine Hydrochloride)

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Drug Information of Phentermine Hydrochloride

Product NDC: 51224-202
Proprietary Name: Phentermine Hydrochloride
Non Proprietary Name: Phentermine Hydrochloride
Active Ingredient(s): 30    mg/1 & nbsp;   Phentermine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Phentermine Hydrochloride

Product NDC: 51224-202
Labeler Name: TAGI Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202248
Marketing Category: ANDA
Start Marketing Date: 20130416

Package Information of Phentermine Hydrochloride

Package NDC: 51224-202-50
Package Description: 100 CAPSULE in 1 BOTTLE (51224-202-50)

NDC Information of Phentermine Hydrochloride

NDC Code 51224-202-50
Proprietary Name Phentermine Hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE (51224-202-50)
Product NDC 51224-202
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phentermine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130416
Marketing Category Name ANDA
Labeler Name TAGI Pharma, Inc.
Substance Name PHENTERMINE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]

Complete Information of Phentermine Hydrochloride


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